Modelling of classification rules on metabolic patterns including machine learning and expert knowledge
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Christian Böhm | Christian Baumgartner | Daniela Baumgartner | C. Böhm | C. Baumgartner | D. Baumgartner
[1] Bernhard Liebl,et al. Expanded newborn screening in Bavaria: tracking to achieve requested repeat testing. , 2002, Preventive medicine.
[2] Christian Baumgartner,et al. Classification on high dimensional metabolic data: Phenylketonuria as an example , 2004 .
[3] Pedro Mendes,et al. Emerging bioinformatics for the metabolome , 2002, Briefings Bioinform..
[4] C. Scriver,et al. The Metabolic and Molecular Bases of Inherited Disease, 8th Edition 2001 , 2001, Journal of Inherited Metabolic Disease.
[5] Xiwu Lin,et al. Megavariate data analysis of mass spectrometric proteomics data using latent variable projection method , 2003, Proteomics.
[6] I. Matsumoto,et al. Advances in chemical diagnosis and treatment of metabolic disorders , 1992 .
[7] Thomas G. Dietterich. What is machine learning? , 2020, Archives of Disease in Childhood.
[8] Antonio Rodríguez-Fernández,et al. Prenatal and post-natal imaging of an hepatic mesenchymal hamartoma , 2002, European Journal of Pediatrics.
[9] S. Amladi,et al. Online Mendelian Inheritance in Man 'OMIM'. , 2003, Indian journal of dermatology, venereology and leprology.
[10] D H Chace,et al. Laboratory integration and utilization of tandem mass spectrometry in neonatal screening: a model for clinical mass spectrometry in the next millennium , 1999, Acta paediatrica (Oslo, Norway : 1992). Supplement.
[11] Russ Wolfinger,et al. Generalizable mass spectrometry mining used to identify disease state biomarkers from blood serum , 2003, Proteomics.
[12] M. Bucknall,et al. Diagnosis of Inborn Errors of Metabolism from Blood Spots by Acylcarnitines and Amino Acids Profiling Using Automated Electrospray Tandem Mass Spectrometry , 1995, Pediatric Research.
[13] D. Millington,et al. Rapid diagnosis of phenylketonuria by quantitative analysis for phenylalanine and tyrosine in neonatal blood spots by tandem mass spectrometry. , 1993, Clinical chemistry.
[14] Bernhard Liebl,et al. Data required for the evaluation of newborn screening programmes , 2003, European Journal of Pediatrics.
[15] G C Cunningham,et al. Use of phenylalanine-to-tyrosine ratio determined by tandem mass spectrometry to improve newborn screening for phenylketonuria of early discharge specimens collected in the first 24 hours. , 1998, Clinical chemistry.
[16] Ian H. Witten,et al. Data mining: practical machine learning tools and techniques, 3rd Edition , 1999 .
[17] Ian H. Witten,et al. Data mining: practical machine learning tools and techniques with Java implementations , 2002, SGMD.
[18] P. Langley. Selection of Relevant Features in Machine Learning , 1994 .
[19] Y. T. Chen,et al. Medium-chain acyl-CoA dehydrogenase (MCAD) deficiency: diagnosis by acylcarnitine analysis in blood. , 1993, American journal of human genetics.
[20] David M. Rocke,et al. Discriminant models for high‐throughput proteomics mass spectrometer data , 2003, Proteomics.
[21] Christian Böhm,et al. Supervised machine learning techniques for the classification of metabolic disorders in newborns , 2004, Bioinform..
[22] Joel Charrow,et al. Tandem mass spectrometry in newborn screening: American College of Medical Genetics/American Society of Human Genetics Test and Technology Transfer Committee Working Group , 2000, Genetics in Medicine.
[23] David W. Hosmer,et al. Applied Logistic Regression , 1991 .
[24] C. Heizmann,et al. Suspected pterin-4a-carbinolamine dehydratase deficiency: Hyperphenylalaninaemia due to inhibition of phenylalanine hydroxylase by tetrahydro-7-biopterin , 1992, Journal of Inherited Metabolic Disease.
[25] Laura A Stokowski. Tandem mass spectrometry in newborn screening. , 2003, Advances in neonatal care : official journal of the National Association of Neonatal Nurses.
[26] J. Ross Quinlan,et al. Induction of Decision Trees , 1986, Machine Learning.
[27] Andreas D. Baxevanis,et al. Searching Online Mendelian Inheritance in Man (OMIM) for Information for Genetic Loci Involved in Human Disease , 2002, Current protocols in human genetics.
[28] T. Suormala,et al. Isolated biotin-resistant deficiency of 3-methylcrotonyl-CoA carboxylase presenting as a clinically severe form in a newborn with fatal outcome , 1992, Journal of Inherited Metabolic Disease.
[29] L. Ohno-Machado. Journal of Biomedical Informatics , 2001 .